Catalog Number

-

Brand Name

ValuLine

Version/Model Number

4756-383

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FRG

Product Code Name

Wrap, Sterilization

Public Device Record Key

f07d787e-b905-44f4-8726-d12a1236b803

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

10366975003024

Quantity per Package

10

Contains DI Package

00366975003027

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case